Abstract
Culture of isolated mouse pancreatic islets in RPMI 1640 for 4 wk with maintenance of specific functions is possible, although a considerable reduction of the number of surviving islets was observed. Culture in medium TC 199 resulted in a lower islet loss, but such islets were functionally less competent. Noncultured C57BL/6J (H-2b) islets were rapidly rejected when allografted intrasplenically into alloxan-diabetic but nonimmunosuppressed C57BL/KsJ (H-2d) mice. By contrast, the immunogenicity of C57BL/6J islets cultured for 4 wk at 37 degrees C in RPMI 1640 and an air-carbon dioxide atmosphere was markedly reduced as evidenced by their ability to partly or completely normalize the hyperglycemia of nonimmunosuppressed alloxan-diabetic C57BL/KsJ mice for several weeks. Both intact islets and islets undergoing rejection were found in the spleens. The present data suggest that in vitro culture for 4 wk may reduce the immunogenicity of the islets, although a complete suppression is not achieved.
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